Species | Lichtheimia corymbifera | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Lineage | Mucoromycota; Mucoromycetes; ; Lichtheimiaceae; Lichtheimia; Lichtheimia corymbifera | |||||||||||
CAZyme ID | CDH56034.1 | |||||||||||
CAZy Family | GT15 | |||||||||||
CAZyme Description | beta--mannosyltransferase | |||||||||||
CAZyme Property |
|
|||||||||||
Genome Property |
|
|||||||||||
Gene Location |
EC | 2.4.1.142:10 | 2.4.1.-:1 |
---|
Family | Start | End | Evalue | family coverage |
---|---|---|---|---|
GT33 | 37 | 452 | 4.1e-137 | 0.9882352941176471 |
Cdd ID | Domain | E-Value | qStart | qEnd | sStart | sEnd | Domain Description |
---|---|---|---|---|---|---|---|
340843 | GT33_ALG1-like | 1.09e-161 | 33 | 455 | 1 | 411 | chitobiosyldiphosphodolichol beta-mannosyltransferase and similar proteins. This family is most closely related to the GT33 family of glycosyltransferases. The yeast gene ALG1 has been shown to function as a mannosyltransferase that catalyzes the formation of dolichol pyrophosphate (Dol-PP)-GlcNAc2Man from GDP-Man and Dol-PP-Glc-NAc2, and participates in the formation of the lipid-linked precursor oligosaccharide for N-glycosylation. In humans ALG1 has been associated with the congenital disorders of glycosylation (CDG) designated as subtype CDG-Ik. |
215155 | PLN02275 | 1.77e-135 | 32 | 420 | 1 | 371 | transferase, transferring glycosyl groups |
223515 | RfaB | 1.73e-09 | 134 | 454 | 86 | 377 | Glycosyltransferase involved in cell wall bisynthesis [Cell wall/membrane/envelope biogenesis]. |
340825 | GT4_WbuB-like | 1.11e-08 | 46 | 433 | 12 | 372 | Escherichia coli WbuB and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. WbuB in E. coli is involved in the biosynthesis of the O26 O-antigen. It has been proposed to function as an N-acetyl-L-fucosamine (L-FucNAc) transferase. |
340816 | Glycosyltransferase_GTB-type | 3.61e-08 | 283 | 406 | 115 | 235 | glycosyltransferase family 1 and related proteins with GTB topology. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. The structures of the formed glycoconjugates are extremely diverse, reflecting a wide range of biological functions. The members of this family share a common GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End |
---|---|---|---|---|---|
7.72e-311 | 1 | 470 | 14 | 502 | |
3.87e-95 | 25 | 454 | 25 | 495 | |
6.21e-94 | 33 | 460 | 41 | 463 | |
2.76e-93 | 40 | 449 | 10 | 450 | |
2.76e-93 | 40 | 449 | 10 | 450 |
Hit ID | E-Value | Query Start | Query End | Hit Start | Hit End | Description |
---|---|---|---|---|---|---|
3.65e-93 | 40 | 449 | 9 | 449 | UDP-glycosyltransferase TURAN OS=Arabidopsis thaliana OX=3702 GN=TUN PE=2 SV=1 |
|
2.19e-91 | 41 | 454 | 38 | 460 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Pongo abelii OX=9601 GN=ALG1 PE=2 SV=1 |
|
6.14e-91 | 41 | 454 | 38 | 460 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Homo sapiens OX=9606 GN=ALG1 PE=1 SV=2 |
|
3.17e-89 | 40 | 467 | 37 | 466 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Mus musculus OX=10090 GN=Alg1 PE=1 SV=3 |
|
2.28e-86 | 40 | 451 | 29 | 416 | Chitobiosyldiphosphodolichol beta-mannosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) OX=284812 GN=alg1 PE=3 SV=2 |
Other | SP_Sec_SPI | CS Position |
---|---|---|
0.994774 | 0.005250 |
Copyright 2022 © YIN LAB, UNL. All rights reserved. Designed by Jinfang Zheng and Boyang Hu. Maintained by Yanbin Yin.